BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL8108

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623270·PEEK Corp Core, Ø12x37mm

    COPIOS BONE VOID FILLER SPONGE AND PASTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FMS VUE II Fluid Management and Tissue Debridement System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020

    GENTLEPOWR LUX CONTRA ANGLE 25LPA

    FDA Adverse Event
    Injury ·KAVO AMERICA·Product code EFB·June 20, 2007

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 26, 2011

    OXYGEN AND AEROSOL THERAPY

    FDA Adverse Event
    Injury ·UNOMEDICAL S.A. DE C.V.·Product code BYG·July 9, 2014

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·EES-JUAREZ·Product code GAG·March 7, 1997

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology